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The study was conducted in accordance with Good Clinical Practice, Declaration of Helsinki (V.1996) and applicable local regulations.
The study will be conducted in France and in Belgium in accordance with Good Clinical Practice, Declaration of Helsinki 2002, validated by the ethical committee (Comité de Protection des Personnes - Ile de France IV, IRB n°00003835. Comission d'éthique biomédicale hospitalo-facultaire de l'hôpital de Louvain, IRB n°B403201213352) and was registed on ClinicalTrials.gov (NCT01367093).
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The study adhered to Good Clinical Practice, the Declaration of Helsinki and all applicable regulations.
The trial is being conducted in accordance with Good Clinical Practice, and Declaration of Helsinki.
The study was conducted in accordance with Good Clinical Practice, the Declaration of Helsinki and local regulations.
The study was conducted according to Good Clinical Practice, the Declaration of Helsinki and applicable rules and regulations of Taiwan and Singapore.
The study was designed and carried out in accordance with good clinical practice, the declaration of Helsinki and national laws.
The study was conducted in accordance with good clinical practice, the Declaration of Helsinki, and appropriate regulatory guidelines.
The guidelines of Good Clinical Practice, the Declaration of Helsinki and other applicable regulatory requirements were adhered to during the conduct of the study.
The study is being conducted in accordance with FDA regulations, the International Conference on Harmonization E6 Guidelines for Good Clinical Practice, the Declaration of Helsinki, and applicable local laws.
The study was reviewed by the hospital ethical committee and was carried out in accordance to Good Clinical Practice and Declaration of Helsinki.
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